Canonical Allele Identifier: CA1714178851

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66638967A= , CM000669.2:g.66638967A=	GRCh38
NC_000007.13:g.66103954A= , CM000669.1:g.66103954A=	GRCh37
NC_000007.12:g.65741389A=	NCBI36
NG_028110.1:g.15087A=
NG_028110.2:g.15087A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.565A=	ENSP00000275532.4:p.Met189=
ENST00000449064.6:c.505+38A=
ENST00000503687.2:c.397+38A=	ENSP00000421074.1:n.397+38A=
ENST00000638524.1:c.430A=
ENST00000638540.1:c.409A=
ENST00000639828.2:c.605A= MANE Select	ENSP00000492240.1:p.Tyr202=
ENST00000639879.1:c.*468A=	ENSP00000492161.1:n.*468A=
ENST00000640234.1:c.437+38A=
ENST00000640385.1:c.605A=	ENSP00000491193.1:p.Tyr202=
ENST00000640601.1:c.112A=
ENST00000640851.1:c.567+38A=	ENSP00000492577.1:n.567+38A=
ENST00000275532.7:c.605A=	ENSP00000275532.3:p.Tyr202=
ENST00000443322.1:c.605A=	ENSP00000411624.1:p.Tyr202=
ENST00000503687.1:c.397+38A=	ENSP00000421074.1:n.397+38A=
NM_001167961.2:c.605A=	NP_001161433.1:p.Tyr202=
NM_153033.4:c.605A=	NP_694578.1:p.Tyr202=
NM_153033.5:c.605A= MANE Select	NP_694578.1:p.Tyr202=